HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395852Erstellt: 24. Oktober 2026
Toluene → N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide
https://huagongshe.com/de/reaction/395852
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Toluene | HCID 1140 | — |
| Edukt | Phosgene | HCID 6371 | — |
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Edukt | Quinoline | HCID 7047 | — |
| Edukt | 2-amino-N-(4-methoxyphenyl)benzamide | HCID 478820 | — |
| Edukt | 1-(Pyridin-4-yl)piperidin-4-ol | HCID 23447619 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide | HCID 18174418 | 46% |
Reaktionsschritte
To a mixture of 1-(4-pyridyl)-4-hydroxypiperidine (536 mg, 3.01 mmol) and methylene chloride (45 mL) was added methanesulfonic acid (0.2 ml, 3.1 mmol). After stirring for 15 seconds, quinoline (0.45 mL, 3.8 mmol) was added, immediately followed by 1.93 M phosgene in toluene (2 mL, 3.9 mmol). After 5 minutes, the reaction was placed in a 35° C. oil bath for 45 minutes. The reaction was cooled to room temperature and N-(4-methoxyphenyl)-2-aminobenzamide (728 mg, 3.0 mmol) and quinoline(0.45 mL, 3.8 mmol) were added. After stirring overnight, the reaction was diluted with CH2Cl2(150 mL) and washed with sat'd sodium carbonate (2×25 mL). The organic layer was concentrated and the crude residue was chromatographed to give 617 mg (46%) of the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06605626B2 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-2df88400879e4876b1fd1e7676a166ee |
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| Quellennotiz | uspto-grants-2003_08 |
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